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Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

PaperCitations, authors & open-access status

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism is a paper indexed in ScholarIQ from OpenAlex.

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ScholarIQcitation count

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism has 357 citations in the OpenAlex counts ScholarIQ stores.

When was Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism published?

ScholarIQyear

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism has 2015 year in the ScholarIQ index.

What is the open-access status of Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism?

ScholarIQoa status

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism has gold oa status in the ScholarIQ index.

What is the DOI of Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism?

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The OpenAlex for Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism is on the source record.

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